A T cell-independent antitumor response in mice with bone marrow cells retrovirally transduced with an antibody/Fc-gamma chain chimeric receptor gene recognizing a human ovarian cancer antigen

Nat Med. 1998 Feb;4(2):168-72. doi: 10.1038/nm0298-168.


In order to treat common cancers with immunotherapy, chimeric receptors have been developed that combine the tumor specificity of antibodies with T-cell effector functions. Previously, we demonstrated that T cells transduced with a chimeric receptor gene against human ovarian cancer were able to recognize ovarian cancer cells in vitro and in vivo. We now report that recipients of bone marrow cells transduced with these genes exhibited significant antitumor activity in vivo. Moreover, in vivo depletion of T cells in reconstituted mice did not affect antitumor activity, suggesting that other immune cells expressing the chimeric receptor gene may play an important role in tumor rejection.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / genetics
  • Cytokines / metabolism
  • Female
  • Hematopoietic Stem Cell Transplantation / methods*
  • Hematopoietic Stem Cells / virology*
  • Humans
  • Immunoglobulin Variable Region
  • Immunotherapy / methods
  • Mice
  • Mice, Inbred C57BL
  • Neoplasms, Experimental / genetics
  • Neoplasms, Experimental / immunology
  • Ovarian Neoplasms / genetics
  • Radiation Dosage
  • Receptors, Antigen, T-Cell / genetics*
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / pharmacology*
  • Retroviridae / genetics
  • T-Lymphocytes / immunology


  • Antibodies, Monoclonal
  • Cytokines
  • Immunoglobulin Variable Region
  • Receptors, Antigen, T-Cell
  • Recombinant Fusion Proteins